Source: ALL
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs104893922 | 0.925 | 0.080 | 5 | 70946157 | missense variant | A/G | snv | 3 | |||
| rs104893935 | 0.882 | 0.080 | 5 | 70942416 | missense variant | C/G | snv | 3 | |||
| rs141760116 | 0.925 | 0.080 | 5 | 70951939 | splice acceptor variant | A/C;G;T | snv | 4.0E-06 | 3 |